Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Rgs9bptm1Hels
Name:	regulator of G-protein signalling 9 binding protein; targeted mutation 1, Stefan Heller
MGI ID:	MGI:3028628
Synonyms:	R9AP-
Gene:	Rgs9bp  Location: Chr7:35278418-35285007 bp, - strand  Genetic Position: Chr7, 21.37 cM
Alliance:	Rgs9bptm1Hels page

Germline Transmission:	Earliest citation of germline transmission: J:87582
Parent Cell Line:	E14 (ES Cell)
Strain of Origin:	129P2/OlaHsd

Allele Type:    Targeted (Null/knockout, Reporter) Mutation:    Other   Mutation details: The entire, intronless, coding region was replaced with a cassette containing tau-lacZ and neo. Protein was undetected in the retinas of homozygous mutant mice by Western blot analysis. (J:87582)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

1 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Rgs9bp Mutation:	6 strains or lines available

Original:	J:87582 Keresztes G, et al., Absence of the RGS9.Gbeta5 GTPase-activating complex in photoreceptors of the R9AP knockout mouse. J Biol Chem. 2004 Jan 16;279(3):1581-4
All:	10 reference(s)